Porous marine snow differentially benefits chemotactic, motile, and nonmotile bacteria
<jats:title>Abstract</jats:title> <jats:p>Particulate organic carbon settling through the marine water column is a key process that regulates the global climate by sequestering atmospheric carbon. The initial colonization of marine particles by heterotrophic bacteri...
Main Authors: | , , , , |
---|---|
Other Authors: | |
Format: | Article |
Published: |
Oxford University Press (OUP)
2023
|
Online Access: | https://hdl.handle.net/1721.1/148461 |
_version_ | 1826209023730384896 |
---|---|
author | Borer, Benedict Zhang, Irene H Baker, Amy E O'Toole, George A Babbin, Andrew R |
author2 | Massachusetts Institute of Technology. Department of Earth, Atmospheric, and Planetary Sciences |
author_facet | Massachusetts Institute of Technology. Department of Earth, Atmospheric, and Planetary Sciences Borer, Benedict Zhang, Irene H Baker, Amy E O'Toole, George A Babbin, Andrew R |
author_sort | Borer, Benedict |
collection | MIT |
description | <jats:title>Abstract</jats:title>
<jats:p>Particulate organic carbon settling through the marine water column is a key process that regulates the global climate by sequestering atmospheric carbon. The initial colonization of marine particles by heterotrophic bacteria represents the first step in recycling this carbon back to inorganic constituents—setting the magnitude of vertical carbon transport to the abyss. Here, we demonstrate experimentally using millifluidic devices that, although bacterial motility is essential for effective colonization of a particle leaking organic nutrients into the water column, chemotaxis specifically benefits at intermediate and higher settling velocities to navigate the particle boundary layer during the brief window of opportunity provided by a passing particle. We develop an individual-based model that simulates the encounter and attachment of bacterial cells with leaking marine particles to systematically evaluate the role of different parameters associated with bacterial run-and-tumble motility. We further use this model to explore the role of particle microstructure on the colonization efficiency of bacteria with different motility traits. We find that the porous microstructure facilitates additional colonization by chemotactic and motile bacteria, and fundamentally alters the way nonmotile cells interact with particles due to streamlines intersecting with the particle surface.</jats:p> |
first_indexed | 2024-09-23T14:16:27Z |
format | Article |
id | mit-1721.1/148461 |
institution | Massachusetts Institute of Technology |
last_indexed | 2024-09-23T14:16:27Z |
publishDate | 2023 |
publisher | Oxford University Press (OUP) |
record_format | dspace |
spelling | mit-1721.1/1484612023-03-11T03:17:44Z Porous marine snow differentially benefits chemotactic, motile, and nonmotile bacteria Borer, Benedict Zhang, Irene H Baker, Amy E O'Toole, George A Babbin, Andrew R Massachusetts Institute of Technology. Department of Earth, Atmospheric, and Planetary Sciences <jats:title>Abstract</jats:title> <jats:p>Particulate organic carbon settling through the marine water column is a key process that regulates the global climate by sequestering atmospheric carbon. The initial colonization of marine particles by heterotrophic bacteria represents the first step in recycling this carbon back to inorganic constituents—setting the magnitude of vertical carbon transport to the abyss. Here, we demonstrate experimentally using millifluidic devices that, although bacterial motility is essential for effective colonization of a particle leaking organic nutrients into the water column, chemotaxis specifically benefits at intermediate and higher settling velocities to navigate the particle boundary layer during the brief window of opportunity provided by a passing particle. We develop an individual-based model that simulates the encounter and attachment of bacterial cells with leaking marine particles to systematically evaluate the role of different parameters associated with bacterial run-and-tumble motility. We further use this model to explore the role of particle microstructure on the colonization efficiency of bacteria with different motility traits. We find that the porous microstructure facilitates additional colonization by chemotactic and motile bacteria, and fundamentally alters the way nonmotile cells interact with particles due to streamlines intersecting with the particle surface.</jats:p> 2023-03-10T17:45:03Z 2023-03-10T17:45:03Z 2022-12-26 Article http://purl.org/eprint/type/JournalArticle 2752-6542 https://hdl.handle.net/1721.1/148461 Borer, Benedict, Zhang, Irene H, Baker, Amy E, O'Toole, George A and Babbin, Andrew R. 2022. "Porous marine snow differentially benefits chemotactic, motile, and nonmotile bacteria." 2 (2). 10.1093/pnasnexus/pgac311 Creative Commons Attribution-NonCommercial-NoDerivs License http://creativecommons.org/licenses/by-nc-nd/4.0/ application/pdf Oxford University Press (OUP) Oxford University Press |
spellingShingle | Borer, Benedict Zhang, Irene H Baker, Amy E O'Toole, George A Babbin, Andrew R Porous marine snow differentially benefits chemotactic, motile, and nonmotile bacteria |
title | Porous marine snow differentially benefits chemotactic, motile, and nonmotile bacteria |
title_full | Porous marine snow differentially benefits chemotactic, motile, and nonmotile bacteria |
title_fullStr | Porous marine snow differentially benefits chemotactic, motile, and nonmotile bacteria |
title_full_unstemmed | Porous marine snow differentially benefits chemotactic, motile, and nonmotile bacteria |
title_short | Porous marine snow differentially benefits chemotactic, motile, and nonmotile bacteria |
title_sort | porous marine snow differentially benefits chemotactic motile and nonmotile bacteria |
url | https://hdl.handle.net/1721.1/148461 |
work_keys_str_mv | AT borerbenedict porousmarinesnowdifferentiallybenefitschemotacticmotileandnonmotilebacteria AT zhangireneh porousmarinesnowdifferentiallybenefitschemotacticmotileandnonmotilebacteria AT bakeramye porousmarinesnowdifferentiallybenefitschemotacticmotileandnonmotilebacteria AT otoolegeorgea porousmarinesnowdifferentiallybenefitschemotacticmotileandnonmotilebacteria AT babbinandrewr porousmarinesnowdifferentiallybenefitschemotacticmotileandnonmotilebacteria |